IP Library Granted Patent US 11,826,417
Granted Patent B2
US 11,826,417 · App. 17/986,424 · Granted Nov 28, 2023

Methods and compositions for producing an adenovirus vector for use with multiple vaccinations

Inventors: Joseph P. Balint (Seattle, WA); Frank R. Jones (Seattle, WA); Richard B. Gayle, III (Seattle, WA)
Assignee: Etubics Corporation
A61K39/12A61K38/191A61K38/193A61K38/204A61K38/208A61K38/2013A61K38/2026A61K38/2033A61K38/2046A61K38/2066A61K38/217A61K39/00A61K39/0011A61K39/001106A61K39/001182A61K39/21A61K39/235A61P35/00C07K14/005C07K14/70503C07K14/71C12N15/86A61K2039/5256A61K2039/54A61K2039/545A61K2039/55555A61K2039/57A61K2039/575C12N2710/10034C12N2710/10321C12N2710/10334C12N2710/10343C12N2710/10371C12N2710/20034C12N2740/15034C12N2740/16234C12N2800/24
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 11,826,417
App. No.
17/986,424
Granted
Nov 28, 2023
Kind
B2
Abstract

Methods for generating immune responses using adenovirus vectors that allow multiple vaccinations with the same adenovirus vector and vaccinations in individuals with preexisting immunity to adenovirus are provided.

Claims (19)

1. A method of treatment for infectious disease or cancer, the method comprising administering an effective amount of a replication defective adenovirus vector two or more times to an individual suffering from or at risk from suffering from infectious disease or cancer, wherein the adenoviral vector comprises 1) a deletion in the E2b region and 2) a nucleic acid sequence encoding one or more target antigens, wherein the target antigens comprise infectious disease or cancer associated proteins.

2. The method of claim 1 , wherein the replication defective adenovirus vector further comprises a deletion in the E1 region.

3. The method of claim 1 , wherein the nucleic acid sequence encoding the antigen is located in the E1 region.

4. The method of claim 1 , wherein the replication defective adenovirus vector further comprises a deletion in the E3 region.

5. The method of claim 1 , wherein the replication defective adenovirus vector is derived from Adenovirus serotype 5.

6. The method of claim 1 , wherein the replication defective adenovirus vector is administered at a concentration of at least 10 10 virus particles/ml.

7. The method of claim 1 , wherein the replication defective adenovirus vector is readministered at least once to the individual.

8. The method of claim 1 , wherein the adenovirus vector is administered 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, or more times.

9. The method of claim 1 , wherein the adenovirus vector is administered intranasally, orally, or via intramuscular, subcutaneous, or intradermal injection.

10. The method of claim 1 , wherein the method comprises administering the replication defective adenovirus vector at a concentration of at least 10 10 virus particles.

11. The method of claim 1 , further comprising administering a second replication defective adenovirus vector comprising a deletion in the E2b region and a nucleic acid sequence encoding an adjuvant.

12. The method of claim 1 , where the individual is further treated with one or more immunostimulants.

13. The method of claim 12 , wherein the immunostimulant is a cytokine.

14. The method of claim 1 , wherein the effective amount is an amount of the adenovirus vector that, when administered, is capable of promoting an immune response in the individual to the one or more target antigens.

15. The method of claim 14 , wherein the target antigen immune response in the individual is monitored to determine the efficacy of the vaccine treatment.

16. The method of claim 15 , wherein the target antigen immune response is monitored by measuring target antigen antibody levels in the individual.

17. The method of claim 15 , wherein the target antigen immune response is monitored by determining levels in the individual of vaccine-dependent cytolytic effector cells capable of killing patient tumor or infected cells in vitro.

18. The method of claim 1 , wherein the target antigen encoded by the adenovirus vector is derived from an infectious organism.

19. The method of claim 1 , wherein the target antigen encoded by the adenovirus vector is derived from a cancer cell.

Assignments (2)
SECURITY INTEREST Recorded Jan 2, 2024
From: IMMUNITYBIO, INC.; NANTCELL, INC.; RECEPTOME, INC.; VBC HOLDINGS LLC; ALTOR BIOSCIENCE, LLC; ETUBICS CORPORATION; IGDRASOL, INC.
To: INFINITY SA LLC, AS PURCHASER AGENT
Reel/Frame 066179/0074 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 9, 2023
From: BALINT, JOSEPH P.; JONES, FRANK R.; GAYLE, RICHARD B., III
To: ETUBICS CORPORATION
Reel/Frame 062638/0567 →
Continuity (7)
Continuation 17881131 · Aug 4, 2022
Continuation 17731106 · Apr 27, 2022
Division 13622263 · Sep 18, 2012
Continuation 12651836 · Jan 4, 2010
Continuation In Part PCTUS2008068924 · Jul 1, 2008
Provisional Application 60947601 · Jul 2, 2007
Related Publication 20230070595A1 · Mar 9, 2023
Cited By (1)
US 12,370,250